An NT (Nuchal Translucency) Scan is a specialized ultrasound performed between 11–14 weeks of pregnancy to assess the baby’s early development and screen for chromosomal conditions. During this scan, the clear space at the back of the baby’s neck—known as the nuchal translucency—is measured, as an increased thickness can indicate a higher chance of genetic conditions such as Down syndrome, Trisomy 18, or Trisomy 13. The scan also helps evaluate the baby’s heartbeat, physical structures, and overall growth at this stage. It is a safe, non-invasive procedure that provides valuable information for early pregnancy care and helps parents make informed decisions. The NT scan is often combined with maternal blood tests for more accurate risk assessment. The procedure is quick, comfortable, and typically completed within a few minutes using high-resolution ultrasound technology. No special preparation is required, although arriving with a comfortably full bladder can sometimes improve imaging clarity.